JP2015509983A5 - - Google Patents
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- JP2015509983A5 JP2015509983A5 JP2015500493A JP2015500493A JP2015509983A5 JP 2015509983 A5 JP2015509983 A5 JP 2015509983A5 JP 2015500493 A JP2015500493 A JP 2015500493A JP 2015500493 A JP2015500493 A JP 2015500493A JP 2015509983 A5 JP2015509983 A5 JP 2015509983A5
- Authority
- JP
- Japan
- Prior art keywords
- item
- pharmaceutically acceptable
- solvate
- ester
- acceptable salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 54
- 150000002148 esters Chemical class 0.000 claims description 35
- 150000003839 salts Chemical class 0.000 claims description 35
- 239000012453 solvate Substances 0.000 claims description 35
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 13
- 229910052794 bromium Inorganic materials 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 229910052740 iodine Inorganic materials 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 claims description 3
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 3
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 description 37
- 239000003814 drug Substances 0.000 description 10
- 229940124597 therapeutic agent Drugs 0.000 description 10
- 0 *[C@@]([C@@]1*)[C@@](CO*)O[C@@]1(*)c1cnc2[n]1N=C(*)NC2* Chemical compound *[C@@]([C@@]1*)[C@@](CO*)O[C@@]1(*)c1cnc2[n]1N=C(*)NC2* 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 208000009620 Orthomyxoviridae Infections Diseases 0.000 description 4
- 208000015181 infectious disease Diseases 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- UBCHPRBFMUDMNC-UHFFFAOYSA-N 1-(1-adamantyl)ethanamine Chemical compound C1C(C2)CC3CC2CC1(C(N)C)C3 UBCHPRBFMUDMNC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 102000014150 Interferons Human genes 0.000 description 2
- 108010050904 Interferons Proteins 0.000 description 2
- QNRRHYPPQFELSF-CNYIRLTGSA-N Laninamivir Chemical compound OC[C@@H](O)[C@@H](OC)[C@@H]1OC(C(O)=O)=C[C@H](N=C(N)N)[C@H]1NC(C)=O QNRRHYPPQFELSF-CNYIRLTGSA-N 0.000 description 2
- 102000005348 Neuraminidase Human genes 0.000 description 2
- 108010006232 Neuraminidase Proteins 0.000 description 2
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 108010093857 Viral Hemagglutinins Proteins 0.000 description 2
- 239000000048 adrenergic agonist Substances 0.000 description 2
- 229940126157 adrenergic receptor agonist Drugs 0.000 description 2
- 102000015395 alpha 1-Antitrypsin Human genes 0.000 description 2
- 108010050122 alpha 1-Antitrypsin Proteins 0.000 description 2
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 description 2
- 229960003805 amantadine Drugs 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 102000016966 beta-2 Adrenergic Receptors Human genes 0.000 description 2
- 108010014499 beta-2 Adrenergic Receptors Proteins 0.000 description 2
- 229940124630 bronchodilator Drugs 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000812 cholinergic antagonist Substances 0.000 description 2
- 239000003246 corticosteroid Substances 0.000 description 2
- 239000003172 expectorant agent Substances 0.000 description 2
- ZCGNOVWYSGBHAU-UHFFFAOYSA-N favipiravir Chemical compound NC(=O)C1=NC(F)=CNC1=O ZCGNOVWYSGBHAU-UHFFFAOYSA-N 0.000 description 2
- 229950008454 favipiravir Drugs 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 210000004969 inflammatory cell Anatomy 0.000 description 2
- 229940079322 interferon Drugs 0.000 description 2
- 229940126181 ion channel inhibitor Drugs 0.000 description 2
- 229950004244 laninamivir Drugs 0.000 description 2
- UKTIJASCFRNWCB-RMIBSVFLSA-N laninamivir octanoate hydrate Chemical compound CCCCCCCC(=O)OC[C@@H](O)[C@@H](OC)[C@@H]1OC(C(O)=O)=C[C@H](N=C(N)N)[C@H]1NC(C)=O UKTIJASCFRNWCB-RMIBSVFLSA-N 0.000 description 2
- 229950005327 laninamivir octanoate hydrate Drugs 0.000 description 2
- 229940066491 mucolytics Drugs 0.000 description 2
- 108700013356 oplunofusp Proteins 0.000 description 2
- VSZGPKBBMSAYNT-RRFJBIMHSA-N oseltamivir Chemical compound CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1 VSZGPKBBMSAYNT-RRFJBIMHSA-N 0.000 description 2
- 229960003752 oseltamivir Drugs 0.000 description 2
- XRQDFNLINLXZLB-CKIKVBCHSA-N peramivir Chemical compound CCC(CC)[C@H](NC(C)=O)[C@@H]1[C@H](O)[C@@H](C(O)=O)C[C@H]1NC(N)=N XRQDFNLINLXZLB-CKIKVBCHSA-N 0.000 description 2
- 229960001084 peramivir Drugs 0.000 description 2
- 239000000651 prodrug Chemical group 0.000 description 2
- 229940002612 prodrug Drugs 0.000 description 2
- 230000000770 proinflammatory effect Effects 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- UGGITRSRFHZMKU-WEIZIPMPSA-N radavirsen Chemical compound N1([C@H]2CN(C[C@H](O2)COP(=O)(N(C)C)N2CCN(CC2)C(=O)OCCOCCOCCO)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CN(C2)P(=O)(OC[C@H]2O[C@H](CNC2)N2C(NC(=O)C(C)=C2)=O)N(C)C)N2C(NC(=O)C(C)=C2)=O)N(C)C)N2C(NC(=O)C(C)=C2)=O)N2CCNCC2)N2C(N=C(N)C=C2)=O)N(C)C)N2C(NC(=O)C(C)=C2)=O)N(C)C)N2C3=NC=NC(N)=C3N=C2)N(C)C)N2C(N=C(N)C=C2)=O)N(C)C)N2C(NC(=O)C(C)=C2)=O)N2CCNCC2)N2C(N=C(N)C=C2)=O)N(C)C)N2C3=NC=NC(N)=C3N=C2)N(C)C)N2C3=C(C(NC(N)=N3)=O)N=C2)N(C)C)N2C3=NC=NC(N)=C3N=C2)N(C)C)N2C3=NC=NC(N)=C3N=C2)N(C)C)N2C3=C(C(NC(N)=N3)=O)N=C2)N(C)C)N2C3=NC=NC(N)=C3N=C2)N(C)C)N2C(NC(=O)C(C)=C2)=O)N2CCNCC2)N2C(NC(=O)C(C)=C2)=O)N(C)C)N2C3=C(C(NC(N)=N3)=O)N=C2)N(C)C)N2C3=C(C(NC(N)=N3)=O)N=C2)N(C)C)C=CC(N)=NC1=O UGGITRSRFHZMKU-WEIZIPMPSA-N 0.000 description 2
- 229960000329 ribavirin Drugs 0.000 description 2
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 description 2
- 229960000888 rimantadine Drugs 0.000 description 2
- 239000003730 rna directed rna polymerase inhibitor Substances 0.000 description 2
- 230000011664 signaling Effects 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 2
- 230000003612 virological effect Effects 0.000 description 2
- 229960001028 zanamivir Drugs 0.000 description 2
- ARAIBEBZBOPLMB-UFGQHTETSA-N zanamivir Chemical compound CC(=O)N[C@@H]1[C@@H](N=C(N)N)C=C(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO ARAIBEBZBOPLMB-UFGQHTETSA-N 0.000 description 2
- 241000712431 Influenza A virus Species 0.000 description 1
- 241000713196 Influenza B virus Species 0.000 description 1
- 241000713297 Influenza C virus Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 108060004795 Methyltransferase Proteins 0.000 description 1
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 description 1
- VYTMBMLLTQRIFQ-GBNDHIKLSA-N N/C(/c1ncc([C@@H]([C@@H]2F)O[C@H](CO)[C@H]2O)[nH]1)=N/C(N)=N Chemical compound N/C(/c1ncc([C@@H]([C@@H]2F)O[C@H](CO)[C@H]2O)[nH]1)=N/C(N)=N VYTMBMLLTQRIFQ-GBNDHIKLSA-N 0.000 description 1
- OVEMXIFZUWQYFQ-GBNDHIKLSA-O NC(NC(c1ncc([C@@H]([C@@H]2F)O[C@H](CO)[C@H]2O)[nH]1)=O)=[NH2+] Chemical compound NC(NC(c1ncc([C@@H]([C@@H]2F)O[C@H](CO)[C@H]2O)[nH]1)=O)=[NH2+] OVEMXIFZUWQYFQ-GBNDHIKLSA-O 0.000 description 1
- KZBZJHYUYNFNGZ-JWMKEVCDSA-N NC1=NC(N)=NN2C1=NCC2[C@@H]([C@@H]1F)O[C@H](CO)[C@H]1O Chemical compound NC1=NC(N)=NN2C1=NCC2[C@@H]([C@@H]1F)O[C@H](CO)[C@H]1O KZBZJHYUYNFNGZ-JWMKEVCDSA-N 0.000 description 1
- 241000712464 Orthomyxoviridae Species 0.000 description 1
- 229940065524 anticholinergics inhalants for obstructive airway diseases Drugs 0.000 description 1
- 239000000168 bronchodilator agent Substances 0.000 description 1
- 229960001334 corticosteroids Drugs 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000002663 nebulization Methods 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261610411P | 2012-03-13 | 2012-03-13 | |
| US61/610,411 | 2012-03-13 | ||
| PCT/US2013/030196 WO2013138236A1 (en) | 2012-03-13 | 2013-03-11 | 2'- substituted carba-nucleoside analogs for antiviral treatment |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017121389A Division JP6525441B2 (ja) | 2012-03-13 | 2017-06-21 | 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015509983A JP2015509983A (ja) | 2015-04-02 |
| JP2015509983A5 true JP2015509983A5 (enExample) | 2016-04-07 |
| JP6242378B2 JP6242378B2 (ja) | 2017-12-06 |
Family
ID=47997868
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015500493A Active JP6242378B2 (ja) | 2012-03-13 | 2013-03-11 | 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体 |
| JP2017121389A Active JP6525441B2 (ja) | 2012-03-13 | 2017-06-21 | 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体 |
| JP2018242679A Withdrawn JP2019069986A (ja) | 2012-03-13 | 2018-12-26 | 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017121389A Active JP6525441B2 (ja) | 2012-03-13 | 2017-06-21 | 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体 |
| JP2018242679A Withdrawn JP2019069986A (ja) | 2012-03-13 | 2018-12-26 | 抗ウイルス処置のための２’−置換カルバヌクレオシド類似体 |
Country Status (18)
| Country | Link |
|---|---|
| US (4) | US9481704B2 (enExample) |
| EP (4) | EP3351552B1 (enExample) |
| JP (3) | JP6242378B2 (enExample) |
| KR (1) | KR102068856B1 (enExample) |
| CN (2) | CN106749272B (enExample) |
| AU (2) | AU2013232378B2 (enExample) |
| CA (1) | CA2866381C (enExample) |
| EA (2) | EA028928B9 (enExample) |
| ES (4) | ES2621217T3 (enExample) |
| IL (2) | IL234586A (enExample) |
| IN (1) | IN2014DN08505A (enExample) |
| MD (1) | MD4496C1 (enExample) |
| MX (1) | MX355267B (enExample) |
| NZ (1) | NZ629996A (enExample) |
| PL (1) | PL2834258T3 (enExample) |
| PT (1) | PT2834258T (enExample) |
| SI (1) | SI2834258T1 (enExample) |
| WO (1) | WO2013138236A1 (enExample) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG171914A1 (en) | 2008-12-02 | 2011-07-28 | Chiralgen Ltd | Method for the synthesis of phosphorus atom modified nucleic acids |
| US9744183B2 (en) | 2009-07-06 | 2017-08-29 | Wave Life Sciences Ltd. | Nucleic acid prodrugs and methods of use thereof |
| DK2620428T3 (da) | 2010-09-24 | 2019-07-01 | Wave Life Sciences Ltd | Asymmetrisk hjælpegruppe |
| RU2014105311A (ru) | 2011-07-19 | 2015-08-27 | Уэйв Лайф Сайенсес Пте. Лтд. | Способы синтеза функционализованных нуклеиновых кислот |
| US8633198B1 (en) | 2011-09-20 | 2014-01-21 | Nant Holdings Ip, Llc | Small molecule inhibitors of influenza A RNA-dependent RNA polymerase |
| CA3107640A1 (en) | 2011-12-22 | 2013-06-27 | Janssen Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof and their use in ameliorating or treating a disease or condition associated with viral infections |
| ES2621217T3 (es) * | 2012-03-13 | 2017-07-03 | Gilead Sciences, Inc. | Análogos de carba-nucleósido 2'-sustituidos para tratamiento antivírico |
| PL2827875T3 (pl) * | 2012-03-21 | 2019-07-31 | Janssen Biopharma, Inc. | Podstawione nukleozydy, nukleotydy i ich analogi |
| US9441007B2 (en) | 2012-03-21 | 2016-09-13 | Alios Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| USRE48171E1 (en) | 2012-03-21 | 2020-08-25 | Janssen Biopharma, Inc. | Substituted nucleosides, nucleotides and analogs thereof |
| PT2872485T (pt) | 2012-07-13 | 2021-03-05 | Wave Life Sciences Ltd | Grupo auxiliar assimétrico |
| UA119050C2 (uk) * | 2013-11-11 | 2019-04-25 | Ґілеад Саєнсиз, Інк. | ПІРОЛО[1.2-f][1.2.4]ТРИАЗИНИ, ЯКІ ВИКОРИСТОВУЮТЬСЯ ДЛЯ ЛІКУВАННЯ РЕСПІРАТОРНО-СИНЦИТІАЛЬНИХ ВІРУСНИХ ІНФЕКЦІЙ |
| CN106232119B (zh) * | 2013-12-11 | 2021-02-19 | 河谷控股Ip有限责任公司 | A型流感rna-依赖性rna聚合酶的小分子抑制剂 |
| PT3094728T (pt) | 2014-01-16 | 2022-05-19 | Wave Life Sciences Ltd | Desenho quiral |
| CA2945693C (en) * | 2014-02-06 | 2020-06-16 | Riboscience Llc | 4'-difluoromethyl substituted nucleoside derivatives as inhibitors of influenza rna replication |
| WO2015143712A1 (en) * | 2014-03-28 | 2015-10-01 | Merck Sharp & Dohme Corp. | 4'-substituted nucleoside reverse transcriptase inhibitors |
| TWI678369B (zh) | 2014-07-28 | 2019-12-01 | 美商基利科學股份有限公司 | 用於治療呼吸道合胞病毒感染之噻吩並［３,２-ｄ］嘧啶、呋喃並［３,２-ｄ］嘧啶及吡咯並［３,２-ｄ］嘧啶化合物類 |
| JP6671355B2 (ja) | 2014-09-26 | 2020-03-25 | リボサイエンス・エルエルシー | 呼吸器多核体ウイルスのｒｎａ複製の阻害剤としての４’‐ビニル置換ヌクレオシド誘導体 |
| SMT202100592T1 (it) | 2014-12-26 | 2021-11-12 | Univ Emory | Derivati antivirali della n4-idrossicitidina |
| RU2720811C2 (ru) | 2015-09-23 | 2020-05-13 | Мерк Шарп И Доум Лимитед | 4'-замещенные нуклеозидные ингибиторы обратной транскриптазы и их получение |
| US10202412B2 (en) | 2016-07-08 | 2019-02-12 | Atea Pharmaceuticals, Inc. | β-D-2′-deoxy-2′-substituted-4′-substituted-2-substituted-N6-substituted-6-aminopurinenucleotides for the treatment of paramyxovirus and orthomyxovirus infections |
| MY199746A (en) | 2017-04-24 | 2023-11-21 | Cocrystal Pharma Inc | Pyrrolopyrimidine derivatives useful as inhibitors of influenza virus replication |
| ES2995458T3 (en) | 2017-12-07 | 2025-02-10 | Univ Emory | N4-hydroxycytidine derivative and anti-viral uses related thereto |
| US11040975B2 (en) | 2017-12-08 | 2021-06-22 | Merck Sharp & Dohme Corp. | Carbocyclic nucleoside reverse transcriptase inhibitors |
| MX2021000917A (es) | 2018-07-27 | 2021-06-23 | Cocrystal Pharma Inc | Derivados de pirrolo[2,3-b]piridina como inhibidores de la replicación del virus de la gripe. |
| ES2937837T3 (es) | 2018-09-10 | 2023-03-31 | Cocrystal Pharma Inc | Inhibidores de piridopirazina y piridotriazina de la replicación del virus de la gripe |
| US20220048897A1 (en) | 2018-11-26 | 2022-02-17 | Cocrystal Pharma, Inc. | Inhibitors of influenza virus replication |
| AR121356A1 (es) | 2020-02-18 | 2022-05-11 | Gilead Sciences Inc | Compuestos antivirales |
| TWI874791B (zh) | 2020-02-18 | 2025-03-01 | 美商基利科學股份有限公司 | 抗病毒化合物 |
| TWI794742B (zh) | 2020-02-18 | 2023-03-01 | 美商基利科學股份有限公司 | 抗病毒化合物 |
| EP4125810A1 (en) * | 2020-03-22 | 2023-02-08 | InspirMed Corp. | Composition of antiviral agent for use in prophylactic or post-exposure treatment of infectious or respiratory diseases |
| AU2021245634A1 (en) * | 2020-03-30 | 2022-10-20 | Fujifilm Toyama Chemical Co., Ltd. | Coronavirus infection treatment drug |
| CN111956630A (zh) * | 2020-08-20 | 2020-11-20 | 大连理工大学 | 一种瑞德西韦供雾化器用的液体制剂、制备方法及其应用 |
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| US12116380B2 (en) | 2021-08-18 | 2024-10-15 | Gilead Sciences, Inc. | Phospholipid compounds and methods of making and using the same |
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